Rare and low-frequency coding genetic variants contribute to pediatric-onset multiple sclerosis.
Mult Scler
; 29(4-5): 505-511, 2023 04.
Article
in En
| MEDLINE
| ID: mdl-36755464
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Multiple Sclerosis
Type of study:
Prognostic_studies
Limits:
Adult
/
Child
/
Humans
Language:
En
Journal:
Mult Scler
Journal subject:
NEUROLOGIA
Year:
2023
Type:
Article
Affiliation country:
United States